Dr Reddy's Q1FY27 Results: Revenue falls 5.6%, margins hit by semaglutide
- Revenue fell 5.6% YoY to ₹8,071 crore due to semaglutide API issues and lower lenalidomide sales
- EBITDA margin contracted to 12.5%, excluding a ₹240 crore provision that would have yielded an ~18% margin
- Underlying base business grew double-digit, with India revenues surging 70% and emerging markets up 31%
- Net cash surplus stands at ₹3,057 crore; full-year capex guidance is ₹1,800 crore
- Management targets resumption of semaglutide supplies by November 2026

*this image is generated using AI for illustrative purposes only.
Dr Reddy's Laboratories reported a 5.6% decline in revenue for Q1FY27, driven by operational disruptions in its semaglutide API business and lower lenalidomide sales. The pharmaceutical major logged consolidated revenue of ₹8,071 crore ($853 million) and net profit of ₹443 crore ($47 million).
Financial Performance
The company’s reported EBITDA margin stood at 12.5%, down from higher levels in prior periods, primarily due to a provision of ₹240 crore related to rejected semaglutide API batches and associated costs. Excluding this provision, management indicated the underlying EBITDA margin would have been approximately 18%. Gross profit margin fell 1,039 bps year-on-year to 46.5%, reflecting the mix shift and higher solvent costs linked to Middle East conflicts.
| Metric | Q1FY27 | Change (YoY) |
|---|---|---|
| Revenue | ₹8,071 crore | -5.6% |
| Net Profit | ₹443 crore | Not specified |
| EBITDA Margin | 12.5% | Negative impact |
| Gross Margin | 46.5% | -1,039 bps |
Operating working capital decreased by ₹81 crore to ₹14,353 crore as of June 30, 2026. The company maintained a net cash surplus of ₹3,057 crore ($323 million). Capital expenditure for the quarter was ₹307 crore ($32 million), with full-year guidance set at approximately ₹1,800 crore.
Business Highlights
Despite the headline revenue decline, the underlying base business delivered double-digit growth across key geographies.
- North America: Revenue fell 41% YoY to $236 million due to lenalidomide declines, but the base business grew double-digit sequentially. The company launched complex generics including bosutinib and nintedanib.
- Emerging Markets: Revenue rose 31% YoY to ₹1,833 crore, driven by new product launches and favorable currency movements.
- India: Domestic revenues surged 70% YoY to ₹1,788 crore, outperforming the Indian pharmaceutical market growth rate of 13.5%. Organic growth in India, excluding recent acquisitions, was 15.5%.
- Europe: Revenue remained broadly flat at $131 million, impacted by price erosion and operating model changes post-NRT integration.
What the Numbers Show
A significant divergence exists between reported profitability and operational performance. While net profit margins appeared compressed at 5.25% (before adjusting for the semaglutide provision), the effective tax rate dropped to 21.3% from 26% in the prior year. This reduction was driven by the reversal of previously recognized tax provisions following favorable resolutions of earlier assessments. Consequently, the headline profit figure masks the severity of the operational hit from the ₹240 crore inventory provision, which disproportionately affected gross and EBITDA margins relative to the tax benefit received.
Strategic Outlook
Management plans to resume semaglutide commercial supplies by November 2026, targeting the delivery of 6–7 million pens between November and March. The company secured approval for semaglutide in Canada for type 2 diabetes treatment. On the regulatory front, the US FDA completed a pre-license inspection at the Bachupally biologics facility, issuing a Form 483 with seven observations, which the company has addressed. Abatacept approval remains targeted for December 2026.
How will the resumption of semaglutide commercial supplies in November 2026 impact Dr. Reddy's revenue trajectory and EBITDA margins in the subsequent quarters?
What are the potential long-term implications of the FDA Form 483 observations at the Bachupally biologics facility on the timeline for abatacept approval and future US regulatory inspections?
Can the double-digit organic growth observed in India and Emerging Markets sustain momentum to offset the significant revenue decline in North America driven by lenalidomide sales?

































